Chenevix-Trench G - Search Results

1

Kinome profiling reveals breast cancer heterogeneity and identifies targeted therapeutic opportunities for triple negative breast cancer.

Al-Ejeh F, Miranda M, Shi W, Simpson PT, Song S, Vargas AC, Saunus JM, Smart CE, Mariasegaram M, Wiegmans AP, Chenevix-Trench G, Lakhani SR, Khanna KK. Al-Ejeh F, et al. Oncotarget. 2014 May 30;5(10):3145-58. doi: 10.18632/oncotarget.1865. Oncotarget. 2014. PMID: 24762669 Free PMC article.

2

Dominant negative ATM mutations in breast cancer families.

Chenevix-Trench G, Spurdle AB, Gatei M, Kelly H, Marsh A, Chen X, Donn K, Cummings M, Nyholt D, Jenkins MA, Scott C, Pupo GM, Dörk T, Bendix R, Kirk J, Tucker K, McCredie MR, Hopper JL, Sambrook J, Mann GJ, Khanna KK. Chenevix-Trench G, et al. J Natl Cancer Inst. 2002 Feb 6;94(3):205-15. doi: 10.1093/jnci/94.3.205. J Natl Cancer Inst. 2002. PMID: 11830610

3

ATM and genome maintenance: defining its role in breast cancer susceptibility.

Khanna KK, Chenevix-Trench G. Khanna KK, et al. J Mammary Gland Biol Neoplasia. 2004 Jul;9(3):247-62. doi: 10.1023/B:JOMG.0000048772.92326.a1. J Mammary Gland Biol Neoplasia. 2004. PMID: 15557798 Review.

4

Low frequency of CHEK2 1100delC allele in Australian multiple-case breast cancer families: functional analysis in heterozygous individuals.

Jekimovs CR, Chen X, Arnold J, Gatei M, Richard DJ, Spurdle AB, Khanna KK, Chenevix-Trench G; kConFab Investigators. Jekimovs CR, et al. Br J Cancer. 2005 Feb 28;92(4):784-90. doi: 10.1038/sj.bjc.6602381. Br J Cancer. 2005. PMID: 15700044 Free PMC article.

5

Characterization of the breast cancer associated ATM 7271T>G (V2424G) mutation by gene expression profiling.

Waddell N, Jonnalagadda J, Marsh A, Grist S, Jenkins M, Hobson K, Taylor M, Lindeman GJ, Tavtigian SV, Suthers G, Goldgar D, Oefner PJ; kConFab Investigators; Taylor D, Grimmond S, Khanna KK, Chenevix-Trench G. Waddell N, et al. Genes Chromosomes Cancer. 2006 Dec;45(12):1169-81. doi: 10.1002/gcc.20381. Genes Chromosomes Cancer. 2006. PMID: 17001622

6

Mutation analysis of five candidate genes in familial breast cancer.

Marsh A, Healey S, Lewis A, Spurdle AB, Kedda MA, Khanna KK; kConFab; Mann GJ, Pupo GM, Lakhani SR, Chenevix-Trench G. Marsh A, et al. Breast Cancer Res Treat. 2007 Nov;105(3):377-89. doi: 10.1007/s10549-006-9461-z. Epub 2006 Dec 23. Breast Cancer Res Treat. 2007. PMID: 17187232

7

A novel corepressor, BCoR-L1, represses transcription through an interaction with CtBP.

Pagan JK, Arnold J, Hanchard KJ, Kumar R, Bruno T, Jones MJ, Richard DJ, Forrest A, Spurdle A, Verdin E, Crossley M, Fanciulli M, Chenevix-Trench G, Young DB, Khanna KK. Pagan JK, et al. J Biol Chem. 2007 May 18;282(20):15248-57. doi: 10.1074/jbc.M700246200. Epub 2007 Mar 22. J Biol Chem. 2007. PMID: 17379597 Free article.

8

BCoR-L1 variation and breast cancer.

Lose F, Arnold J, Young DB, Brown CJ, Mann GJ, Pupo GM; Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer; Khanna KK, Chenevix-Trench G, Spurdle AB. Lose F, et al. Breast Cancer Res. 2007;9(4):R54. doi: 10.1186/bcr1759. Breast Cancer Res. 2007. PMID: 17697391 Free PMC article.

9

Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants?

Lovelock PK, Spurdle AB, Mok MT, Farrugia DJ, Lakhani SR, Healey S, Arnold S, Buchanan D; kConFab Investigators; Couch FJ, Henderson BR, Goldgar DE, Tavtigian SV, Chenevix-Trench G, Brown MA. Lovelock PK, et al. Breast Cancer Res. 2007;9(6):R82. doi: 10.1186/bcr1826. Breast Cancer Res. 2007. PMID: 18036263 Free PMC article.

10

Clinical classification of BRCA1 and BRCA2 DNA sequence variants: the value of cytokeratin profiles and evolutionary analysis--a report from the kConFab Investigators.

Spurdle AB, Lakhani SR, Healey S, Parry S, Da Silva LM, Brinkworth R, Hopper JL, Brown MA, Babikyan D, Chenevix-Trench G, Tavtigian SV, Goldgar DE; kConFab Investigators. Spurdle AB, et al. J Clin Oncol. 2008 Apr 1;26(10):1657-63. doi: 10.1200/JCO.2007.13.2779. J Clin Oncol. 2008. PMID: 18375895

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